ClinVar Miner

Submissions for variant NM_002294.3(LAMP2):c.222T>A (p.Tyr74Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003510013 SCV004317108 pathogenic Danon disease 2023-08-25 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Tyr74*) in the LAMP2 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in LAMP2 are known to be pathogenic (PMID: 21415759). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with LAMP2-related conditions. For these reasons, this variant has been classified as Pathogenic.

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